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Research 151–180 of 1000+
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Monilethrix – Case report of a rare disease
- Management of congenital ichthyoses: European guidelines of care, part two
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- Masquerading of trichotillomania in a family with monilethrix
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Gene Therapy: Recent Advances and Applications in Dermatology
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- Abstracts
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Hair Today
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Gene Delivery to the Hair Follicle
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Report from the Cicatricial Alopecia Colloquium
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- The Epithelial Stem Cell Niche in Skin
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle